Busch Lab

ZMP

flt4

Ensembl ID:
ENSDARG00000015717
ZFIN ID:
ZDB-GENE-980526-326
Description:
Vascular endothelial growth factor receptor 3 [Source:UniProtKB/Swiss-Prot;Acc:Q5MD89]
Human Orthologue:
FLT4
Human Description:
fms-related tyrosine kinase 4 [Source:HGNC Symbol;Acc:3767]
Mouse Orthologue:
Flt4
Mouse Description:
FMS-like tyrosine kinase 4 Gene [Source:MGI Symbol;Acc:MGI:95561]

Alleles

There are 10 alleles of this gene:

Allele Name Consequence Status Availability
sa42378 Nonsense Mutation detected in F1 DNA Not yet available
sa35677 Essential Splice Site Available for shipment Available now
sa9798 Nonsense Available for shipment Available now
sa281 Nonsense F2 line generated Not yet available
sa35676 Nonsense Mutation detected in F1 DNA Not yet available
sa31980 Nonsense Available for shipment Available now
sa44806 Essential Splice Site Mutation detected in F1 DNA Not yet available
sa16036 Nonsense Available for shipment Available now
sa35675 Essential Splice Site Mutation detected in F1 DNA Not yet available
sa30675 Nonsense Mutation detected in F1 DNA Not yet available

Mutation Details

Allele Name:
sa42378
Status:
Mutation detected in F1 DNA
For more information about the meaning of this status and other statuses, please see our FAQs.
Availability:
Not yet available
Mutation:
T > G
Consequence:
Nonsense
Transcripts:
Transcript ID Consequence Amino Acid Affected Amino Acid Total Exon Affected Exon Total
ENSDART00000125081 Nonsense 86 1368 3 30
Genomic Location (Zv9):
Chromosome 14 (position 19820163)
Other Location(s):
Assembly Chromosome Position
GRCz10 14 15614616
GRCz11 14 15920179
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
GAGTTTACTGATCGCCAGGGTCAGCAGTCACCCACTGACACCCCAGGGTA[T/G]AGAGAAATCAGGCTGAAGGAGTGTCAAGGGGTGGCTGGAAAACCCTACTG
Long Flanking Sequence:
ATAATGGCCGAGTTTTCATTTTTGGGTGAACTATTCCTTTAAATGTTTATATGTTTTTTAATCTGCTCCAATATTTGCACAACATCCATAGTGTACTGGTCGGCGTTACTATTTCTTGTCCTGTCTTATTTACACTAAATGTTGCATAAACTGCACTTTGTGCTCTTATTCGTATTTTATTTATTTTTATTTTAGTATATTTTATTTTATTTCATTCTCAAAAATGTTTATAGTAGTGCACTGTCCTGTGTTATGTTGTTAGTTTATGCTGTTTGATGTAGCACCTTGGTCCTGGAGGAACATTGTTTTGTTTCACTGTATACTGCAATGTATATTATTGAAATGACAATAAAGCCGTCTTGACTTGTCTAATGCTTTTATCCGGGCCTTTTCAACAGGGGTCAGCGAATTCTGGACTGGAGCTGGCCTGAAGAGTCTTTGAGTAAAGTGGAGTTTACTGATCGCCAGGGTCAGCAGTCACCCACTGACACCCCAGGGTA[T/G]AGAGAAATCAGGCTGAAGGAGTGTCAAGGGGTGGCTGGAAAACCCTACTGCAAGATCTTAATACTTACCAATGCCCAGGCCAATGACTCGGGTTATTACCGCTGCTTCTACAAGGACATTAAAGCTGTTATTGATGGCACCACGGCAGCCAGCATTTTTGTGTTTGTTCGAGGTAAGAGCTGTGCTGAATGAATATGTTTGTTGTTGTTATGGCATTGTTATTGTCTCTATGCATTCAAAATGTCTTCCAGTTAGTATGACTATGAATCCTTTATTGTTCTTTATGTTAGTCTAGATGTAGTAGTTTCCATTTTTTCACTTTGGGGAATGTGCAACCGAATCGTGCTCCCCATAAAAATGTTAATTTATGTACCATTAGTTCACCCTCAATTTGTTTGAAACATTTACGTGCTTGTTACTTCTATTAAACACAGAAGAAGGTAATTTGATTTTGATGACGTGGTTAACAAATTATCTGAAAGTATTGTCAACATTTGATC
Associated Phenotype:
Not determined

Mutation Details

Allele Name:
sa35677
Status:
Available for shipment
For more information about the meaning of this status and other statuses, please see our FAQs.
Availability:
Order Allele From ZIRC
Mutation:
T > C
Consequence:
Essential Splice Site
Transcripts:
Transcript ID Consequence Amino Acid Affected Amino Acid Total Exon Affected Exon Total
ENSDART00000125081 Essential Splice Site 186 1368 4 30
Genomic Location (Zv9):
Chromosome 14 (position 19804357)
Other Location(s):
Assembly Chromosome Position
GRCz10 14 15598810
GRCz11 14 15904373
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
AGTACCATGTCTGGTTTCAGATCCTGACCTAAAAGTCACTCTCTTCTCGG[T/C]AGGTCTCCAACACGCTTCCAGCAGCAACTCACCTGATCTCTCTGTTTCTG
Long Flanking Sequence:
TTGCGGGTGCCAGTAAGAAGCCTATAGCGGCTGCATTTTTTACCACTTGAAGATTATTTATATAGGAATGGCCAATACCCACATAAATTGAGTTACAGTTGTCCAAGTGTGATGATACAAAGGCATGGATTAATCTCTGGAATTCTGCACGAGTTAAAAAGCCTTTTACTTTGGCTAATAATCTCAGCTGAAAAAAACAAGATCTAACTACTGCATTTACCAATTTGTCAAAAAGAAGGGCAGAGTCTAGGATAAAACAGATTTTTTTTACAGATGGTTGTTGTGTATTGTAATGTGTAAAGGTAACTGAGAAGTAGGTTTCAGAACTTATAGGCAGCTGAACTCATGTGACTTTTTCTTTAAACAAACAGACCCAGAGCATCCATTCATCAAAAGGGGAGACAACGACATGGAGACCATCTTCATAACAGACTCTGAAACACACATCGAAGTACCATGTCTGGTTTCAGATCCTGACCTAAAAGTCACTCTCTTCTCGG[T/C]AGGTCTCCAACACGCTTCCAGCAGCAACTCACCTGATCTCTCTGTTTCTGCAAAATGGATTAGGAGAATCTTTTGTTTTTTGTATTATTTGAGAGGTTTAACTCAGGACTGTTACAGTTACTGCATGCAAAAGTGTAGCTTTCACTCAAGTGACATATGCCTTTCCAAGCCAAAGGAAATGAAAACAGTAACTTAAATAAACAAGTCTTTCTTAAATTTCATCAACATCATTTTTCAGGGAATTTAAATGTGTGGCTTTTGAGTTCACTAGGCCGTGTCAGTGTTGCTGAAATGACAGAAAGTTCTTTTATACTTTGTTAAAGTAAACAGATTTTATCACCTTTGAATAAGTTAAAGTAACTGATTTGATTTATTTTTTTTTCTACCTAAACCAGGGGTCTCAAACTCAATTTACCTGGGGGCCGCAGGAGGCAAAGTCTGGGTGAGGCTGGGCCGCATAAGGGATTTCACAAAAAAAAAAGTCCTCAAATGTCATTATT
Associated Phenotype:
Not determined

Mutation Details

Allele Name:
sa9798
Status:
Available for shipment
For more information about the meaning of this status and other statuses, please see our FAQs.
Availability:
Order Allele From ZIRC
Order Allele From EZRC
Mutation:
T > A
Consequence:
Nonsense
Transcripts:
Transcript ID Consequence Amino Acid Affected Amino Acid Total Exon Affected Exon Total
ENSDART00000125081 Nonsense 563 1368 12 30
Genomic Location (Zv9):
Chromosome 14 (position 19773956)
Other Location(s):
Assembly Chromosome Position
GRCz10 14 15568409
GRCz11 14 15873972
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
YGGCCGTGTGGTTATWCAGAATGCCAGTGTGCCAGCTATGTACAAGTGCT[T/A]GGCTGAGAACAAAGTGGGAAAAGATGAACGACTGATTTATTTCTACGTAA
Long Flanking Sequence:
TCTGAAACTGAAAATATAATGTGAGAAAAGTGGGGGCGAATATGTTACACTGAAATATTTAAACCTATCCCCTAGTCCTTGCTTCCTGGATGGAGAAGGAATAAGCACACATTAACACAGCGTTCTCGTCCTGTTTTCTGTCACACCTGTGAGGTCATTTCCTGTGTGTGGCTTTGGGAATAGGACTGGCAGGGGTGAAAAAGAGAGTATCACAGTATAGTATACAGCTTAAAGTTAGGTCTAGTGTACACCAAAGATTCAATTATTCACTCTTATTTTATCCTAAACCTCTTGAATCCTGTTGTTTTTTCAGTATATAATCTTTTGAGCTCCATATAGAAGAGATAATGCCATGCTGTATGTATTTACTATCTCTTTAATAATGCCTTGCTGTTGTCCAAATGCAAACAAAGCCTAATTGAAAGAGTTTCTGTTGTTCCCATAGACTGTCGGCCGTGTGGTTATTCAGAATGCCAGTGTGCCAGCTATGTACAAGTGCT[T/A]GGCTGAGAACAAAGTGGGAAAAGATGAACGACTGATTTATTTCTACGTAACCAGTGAGTTTCATGCTTTTATGGAAAAAAGTATACACACATGCACACACAAACAATGTAAGCTACAAATCTTGTTTTCATGTTGAAATACGAATATTTTGCTTACCCCGTTGCCAAATTGTTTTACTTGCTTTAAATGGGTGGTCCACCACGATATCATATTTTAAACTTTAGTTGATCTGTAATGTAGTTGTGTGAACAAAAACAACATCTCTGAATGTAATACGCTCAATGCAAGTTCAATGCAAAGGGAGACATTGGCTTTTACAGAGTTAGTTTAGCAAAGCCTACAGCGAATGAAGTTTGGGGACAACAAAAAAAAAAATGCATCCGTGTTAGTGAGATCACAAACACATCAGGTTACGTGCATTCAGCACGTGCACACCCTGCACAGTGAAGGGGCATGGCCAGAGATGCTGTAATGTGGCAGAGAAAGCTAAATGCTGTACA
Associated Phenotype:
Not determined

Mutation Details

Allele Name:
sa281
Status:
F2 line generated
For more information about the meaning of this status and other statuses, please see our FAQs.
Availability:
Not yet available
Mutation:
C > A
Consequence:
Nonsense
Transcripts:
Transcript ID Consequence Amino Acid Affected Amino Acid Total Exon Affected Exon Total
ENSDART00000125081 Nonsense 593 1368 13 30
Genomic Location (Zv9):
Chromosome 14 (position 19772144)
Other Location(s):
Assembly Chromosome Position
GRCz10 14 15566597
GRCz11 14 15872160
KASP Assay ID:
554-2919.1 (used for ordering genotyping assays)
KASP Sequence:
TAACATTCATTTAGCTATCCCTGAAGGATTCGATATAGAGATGGAGCCCT[C/A]AGAGGATCCGCTTGAGCAGGACCTGGTRCAGCTGAAGTGTAATGCAGATA
Long Flanking Sequence:
AAATAACATGACTTTCTACAAATGAAACATGAGAACACATTGCTTTGCATCTTATAAACACAACCAAGCCTTAAAAATACACTCGGGGCCACCCCTTTAAAAAAAAACAACTTAATTTTGACTTTTTACAATAAGACAAGAAAAGACAAGAAAACCATATATTTTTAAAGTTGTGTAGAAAATGTTTCTTGATTTAAGAATTAATGAATATTTGGACTAGAAACAAGACAAAAACTATATATACTTGGTAAACTACAATATATAAAACTATCTATGTAAGAAAAGCATTTTTGCAGCACACACATAAACACACACAAACGCACGCACACACACACACAGACACACGTACAGTATATTTTGGATATTGCTAGTTTAACAGGCTAAACTTAAATTTACATCAATAAAATGGGGTTTCTTGCTGAAGAGATGTGCTGTTACTTCTCTTAATATTAACATTCATTTAGCTATCCCTGAAGGATTCGATATAGAGATGGAGCCCT[C/A]AGAGGATCCGCTTGAGCAGGACCTGGTACAGCTGAAGTGTAATGCAGATAATTTCACCTATGAGAACCTGCGGTGGTACCGCCTGGACCCGCAGACTGTTCCTCCAGAGCTGGACTGCAAGAGTCTGCACCAGTATGCCACATTTTTGGAGGGACAACTATCTTTTCAGACCACCAGCAACAACTGGGTCCTGCAGCTTAACATTACCAACATTCAGCTACAGGATGAGGGGAACTATGTGTGTGAGGTGCAGAACCGACGAACCGGGGTGAAACATTGTCACCGCAAATACATCCCAGTCAAAGGTGAAGGTCAAACAATACTCAACTTTTATTCTGGTAATTTCATTTGCAGTGCGATAAACACTAACTAGCTAAGCTAACTTTTAAAGTAGCATCATAACCTCCACATAACCTTCATTCCGCTGTGGAGACCCCAGAATAATAAAAGGACTAAAGTGAAAAGAAAATGAATGATTGAATGAAAGAACGAATGAGTTT
Associated Phenotype:
Not determined

Mutation Details

Allele Name:
sa35676
Status:
Mutation detected in F1 DNA
For more information about the meaning of this status and other statuses, please see our FAQs.
Availability:
Not yet available
Mutation:
C > T
Consequence:
Nonsense
Transcripts:
Transcript ID Consequence Amino Acid Affected Amino Acid Total Exon Affected Exon Total
ENSDART00000125081 Nonsense 741 1368 14 30
Genomic Location (Zv9):
Chromosome 14 (position 19770417)
Other Location(s):
Assembly Chromosome Position
GRCz10 14 15564870
GRCz11 14 15870433
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
GCACACCCTTTCCTCAGCTGTCCTGGTTTAAAGATAACCAACCCCTCCAT[C/T]AGATATCAGGTTAGTCATTCATCACACTTTTCAATACTAACATTTAAAAG
Long Flanking Sequence:
TAAGGTTAAAATATTTTAATATATGCTGTGAAGATTTACAAAATATTGAAGGGCGAGTTATATTGGAGTGATTTTGCAACTTAAACGTTATCCTGTATGTCAGTTTCAAAACGCACTCAGAAATTACATTTGCTGTTTGTTCAAACTACTTATTTAAAATGAGCTGAAACAAAACGATTGTTTTATTTTTAATCCATTTAAATTTGTAAAAGATAATAAGTGAACTTAATTCCTTCATGTTGTCCCAACACAAATCATTGTATGGAACCCAGGAGTTTTTAAAGTGCATTCTTTTAACAAAGTCAAGAAGGGCAAGCATGTTGTGTAACGTATCACAAATCTCTCTTTTTCTTCATGGCTCAGCAATGGAAGCACCTCGATACCGTCACAACCCAACTAATCATACGGTAAATGTGAGCGAGTCGCTGCAGATGAACTGTGATGTGGAAGGCACACCCTTTCCTCAGCTGTCCTGGTTTAAAGATAACCAACCCCTCCAT[C/T]AGATATCAGGTTAGTCATTCATCACACTTTTCAATACTAACATTTAAAAGTCCAGTGAAATTAAAATAACGTTTTTTAGATATTAGTATCAGTATGTTAATCTTAAGGATATCTATTAGCTAGTGTGGTCTAAAACAGTGACAAAAAAGGCTTTTAGAAGATATAAAATTGATATGAACATGTAAAGATTGTTGTCATTTCCGCCTAAATGAATTCATGTTTATTCCACATAACCTCAAACTTTAGTTTCTCATCAAATCTTGACCAATCAAAGTGCCCTCTGACATGATCTGACATGCCCCACCCCGTTTAATATGCTTTTCATTTGCTTCTCATTTGATGTGATTGAGCTCAACCACTCAATGACAGAGCTGTGATTAAAACAAAACGCCATTGGCTGTTTTTTAAAAGGGGGAGGAGCTACTTTGTATTTTCCTCTCTTTGTGTTTCAGATGAGATAATGTCAAATATTAAATAAAAAAGGATAATTTCAAATGACT
Associated Phenotype:
Not determined

Mutation Details

Allele Name:
sa31980
Status:
Available for shipment
For more information about the meaning of this status and other statuses, please see our FAQs.
Availability:
Order Allele From ZIRC
Mutation:
C > T
Consequence:
Nonsense
Transcripts:
Transcript ID Consequence Amino Acid Affected Amino Acid Total Exon Affected Exon Total
ENSDART00000125081 Nonsense 1031 1368 22 30
Genomic Location (Zv9):
Chromosome 14 (position 19736387)
Other Location(s):
Assembly Chromosome Position
GRCz10 14 15530840
GRCz11 14 15836403
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
AAACTCCACTCACAATAGAGGATCTGATATGCTACAGTTTTCAAGTTGCA[C/T]GAGGAATGGAGTTTCTGGCATCTCGTAAGGTAATTTTCAAACATTTATTT
Long Flanking Sequence:
CTAAATAACCTAGTTTAGCCTTTAATTGTCACTTTAAGCTGTATAGAAATGTCTTGAAAAATATCTAGTGAAATATTATTAACTGTCATCATGGCAAAAATAAAAAAAATCAGTTATTAGAATTTAGTTATTAAAAGTATTATGTTTAGAAATCTGTTGAAAAAGTCTCTCTATTAAACAGAAATTGAGAAAAAAAATAAACAAGGGGGCTAATATTTCAGGGGGGCTAATAATTCTGACTTCAACTGTATATGTTTTAAATGCAAATTTCTGTCACGATTTTGTACCACAACTCATATTTATCCTTAAGATTAGCATACCAACATCTAAAAAACTTTATTTTAATTTCACTGGACCATTAAATGTGCACTTGAATGTGTACTAAAGTTAATAGCAACTATAATGCATTAATAATTTCTCCTTCACCAGTTACAGTGGATGATCTCTGGAAAACTCCACTCACAATAGAGGATCTGATATGCTACAGTTTTCAAGTTGCA[C/T]GAGGAATGGAGTTTCTGGCATCTCGTAAGGTAATTTTCAAACATTTATTTAATCTTAACCTCTGTGATGAATCCTTTATTCAGTTTGTATGTTATTGCTGAACTTTAGATGTTTTAACACTTTATTGCCATCGTAAATGTCTAGTTTACCTTTTGTCTGTAGGTTATCATTTAAAACCTCCTCAAAATTTGTTTGAATTTATTCAAAGAAAGTGGTCAAAAAATTCTTATAGTGAAATTGATTATAAAAAAGAAGGTCATGATGATAAAAAAGGGTTTTGTAAAGCTGGAAGCAAATTGTTACAAATGGCAACAAATAGCCCAGTGTTGCCAGCGTTTTACAACCTTGCACCTTTCACCTCACAAAAGTGTCCTCAGTTACATCTTCCTACAACAGTTTTTATCATTGGTAGAATACACGTTGGTAGAGTAAATTATTTCAACACAGTCATATAAACATAATGATGCAATGTATCAAACCTTTAACCCTTGGAATAAAAA
Associated Phenotype:
Not determined

Mutation Details

Allele Name:
sa44806
Status:
Mutation detected in F1 DNA
For more information about the meaning of this status and other statuses, please see our FAQs.
Availability:
Not yet available
Mutation:
T > A
Consequence:
Essential Splice Site
Transcripts:
Transcript ID Consequence Amino Acid Affected Amino Acid Total Exon Affected Exon Total
ENSDART00000125081 Essential Splice Site 1040 1368 22 30
Genomic Location (Zv9):
Chromosome 14 (position 19736356)
Other Location(s):
Assembly Chromosome Position
GRCz10 14 15530809
GRCz11 14 15836372
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
CTACAGTTTTCAAGTTGCACGAGGAATGGAGTTTCTGGCATCTCGTAAGG[T/A]AATTTTCAAACATTTATTTAATCTTAACCTCTGTGATGAATCCTTTATTC
Long Flanking Sequence:
CTTTAAGCTGTATAGAAATGTCTTGAAAAATATCTAGTGAAATATTATTAACTGTCATCATGGCAAAAATAAAAAAAATCAGTTATTAGAATTTAGTTATTAAAAGTATTATGTTTAGAAATCTGTTGAAAAAGTCTCTCTATTAAACAGAAATTGAGAAAAAAAATAAACAAGGGGGCTAATATTTCAGGGGGGCTAATAATTCTGACTTCAACTGTATATGTTTTAAATGCAAATTTCTGTCACGATTTTGTACCACAACTCATATTTATCCTTAAGATTAGCATACCAACATCTAAAAAACTTTATTTTAATTTCACTGGACCATTAAATGTGCACTTGAATGTGTACTAAAGTTAATAGCAACTATAATGCATTAATAATTTCTCCTTCACCAGTTACAGTGGATGATCTCTGGAAAACTCCACTCACAATAGAGGATCTGATATGCTACAGTTTTCAAGTTGCACGAGGAATGGAGTTTCTGGCATCTCGTAAGG[T/A]AATTTTCAAACATTTATTTAATCTTAACCTCTGTGATGAATCCTTTATTCAGTTTGTATGTTATTGCTGAACTTTAGATGTTTTAACACTTTATTGCCATCGTAAATGTCTAGTTTACCTTTTGTCTGTAGGTTATCATTTAAAACCTCCTCAAAATTTGTTTGAATTTATTCAAAGAAAGTGGTCAAAAAATTCTTATAGTGAAATTGATTATAAAAAAGAAGGTCATGATGATAAAAAAGGGTTTTGTAAAGCTGGAAGCAAATTGTTACAAATGGCAACAAATAGCCCAGTGTTGCCAGCGTTTTACAACCTTGCACCTTTCACCTCACAAAAGTGTCCTCAGTTACATCTTCCTACAACAGTTTTTATCATTGGTAGAATACACGTTGGTAGAGTAAATTATTTCAACACAGTCATATAAACATAATGATGCAATGTATCAAACCTTTAACCCTTGGAATAAAAAACAACACTTTAACAGCACTGAAATACCCAGA
Associated Phenotype:
Not determined

Mutation Details

Allele Name:
sa16036
Status:
Available for shipment
For more information about the meaning of this status and other statuses, please see our FAQs.
Availability:
Order Allele From ZIRC
Order Allele From EZRC
Mutation:
G > A
Consequence:
Nonsense
Transcripts:
Transcript ID Consequence Amino Acid Affected Amino Acid Total Exon Affected Exon Total
ENSDART00000125081 Nonsense 1088 1368 24 30
Genomic Location (Zv9):
Chromosome 14 (position 19733259)
Other Location(s):
Assembly Chromosome Position
GRCz10 14 15527712
GRCz11 14 15833275
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
TTATAGGTGAAGTGTTATCTGTCTTTGCAGGCYAGGCTGCCGCTGAAGTG[G/A]ATGGCTCCAGAGAGCATCTTTGATAARGTTTACACCAGTCAGAGTGACGT
Long Flanking Sequence:
TCAGACACTTTAATCATGTTTTTTTATCCATTCTTTTTATGCAAACCCTGATTAAAAATGAAAAAACTTCACTTATCAAGACCTTTATGGTTACTGATTGTCATTTAAAATATGAGTGTTCTCTTGTACCTTTTTGTTATTTAGATTTCTACATAAAATATGACCTGAACAAACCCCAGCAGAGATTCACCCAACATTTCAGTAAAGGCCAATGGTCAAAAATGAATGCCATTTTTGTCATGGAATAAAGATGTCAGAAATCACATGAAAGGTTGCGAAAACATTTAAAACATCAAATAAAAATCACCTTAAAGCAAAAGTAAGAAGAGCAGGAGTATCACCGCATGACATCCTCATAATGAAGCAGAAAGGTTATGTTTCTGAGACTGAAGCGCTGGAGAATGGCTGCAGATCAGATCAGCTGCAGGATCACGATAAGAGAATTCTCTTTTATAGGTGAAGTGTTATCTGTCTTTGCAGGCCAGGCTGCCGCTGAAGTG[G/A]ATGGCTCCAGAGAGCATCTTTGATAAGGTTTACACCAGTCAGAGTGACGTCTGGTCTTTTGGAGTTCTGCTCTGGGAGATTTTCTCACTAGGTAACAGTTAACCGGGGCAGCTGCAATTAACGCAATGGAGCTGATCAATGGAGTACAATGCACTACAAGAAATACTATTTTAAAATGCAAATTAAAAATTAATAAATGAATAAAAAAAAAAAAAAAAAAAAAAATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATAATGAAATAGTAAGTTAAAAATATAAACAAAAATAGTTCTCCGATTAATTTTCAAGATTTTGGGATGTTGTGTTTTAGTCTGATTTTAAAACAAACCTTTTACTGTCACAATCCAACTAGCAGGACACCTAATTTTAATTAATTCATTCATTCATTCATTCATTCATTTTCTTTTCGGCTTAATCCCTTTATTAATTTGCAGTCGCTA
Associated Phenotype:
Not determined

Mutation Details

Allele Name:
sa35675
Status:
Mutation detected in F1 DNA
For more information about the meaning of this status and other statuses, please see our FAQs.
Availability:
Not yet available
Mutation:
T > C
Consequence:
Essential Splice Site
Transcripts:
Transcript ID Consequence Amino Acid Affected Amino Acid Total Exon Affected Exon Total
ENSDART00000125081 Essential Splice Site 1119 1368 24 30
Genomic Location (Zv9):
Chromosome 14 (position 19733166)
Other Location(s):
Assembly Chromosome Position
GRCz10 14 15527619
GRCz11 14 15833182
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
AGTGACGTCTGGTCTTTTGGAGTTCTGCTCTGGGAGATTTTCTCACTAGG[T/C]AACAGTTAACCGGGGCAGCTGCAATTAACGCAATGGAGCTGATCAATGGA
Long Flanking Sequence:
CTGATTGTCATTTAAAATATGAGTGTTCTCTTGTACCTTTTTGTTATTTAGATTTCTACATAAAATATGACCTGAACAAACCCCAGCAGAGATTCACCCAACATTTCAGTAAAGGCCAATGGTCAAAAATGAATGCCATTTTTGTCATGGAATAAAGATGTCAGAAATCACATGAAAGGTTGCGAAAACATTTAAAACATCAAATAAAAATCACCTTAAAGCAAAAGTAAGAAGAGCAGGAGTATCACCGCATGACATCCTCATAATGAAGCAGAAAGGTTATGTTTCTGAGACTGAAGCGCTGGAGAATGGCTGCAGATCAGATCAGCTGCAGGATCACGATAAGAGAATTCTCTTTTATAGGTGAAGTGTTATCTGTCTTTGCAGGCCAGGCTGCCGCTGAAGTGGATGGCTCCAGAGAGCATCTTTGATAAGGTTTACACCAGTCAGAGTGACGTCTGGTCTTTTGGAGTTCTGCTCTGGGAGATTTTCTCACTAGG[T/C]AACAGTTAACCGGGGCAGCTGCAATTAACGCAATGGAGCTGATCAATGGAGTACAATGCACTACAAGAAATACTATTTTAAAATGCAAATTAAAAATTAATAAATGAATAAAAAAAAAAAAAAAAAAAAAAATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATAATGAAATAGTAAGTTAAAAATATAAACAAAAATAGTTCTCCGATTAATTTTCAAGATTTTGGGATGTTGTGTTTTAGTCTGATTTTAAAACAAACCTTTTACTGTCACAATCCAACTAGCAGGACACCTAATTTTAATTAATTCATTCATTCATTCATTCATTCATTTTCTTTTCGGCTTAATCCCTTTATTAATTTGCAGTCGCTACAGTGGAATGAACCGCCAACTTATCCAGCATCTGTTATACTTAGCTTCCCGCTGCAACCCATCACTGGGAAACACTCATAAACTCTCATTCAA
Associated Phenotype:
Not determined

Mutation Details

Allele Name:
sa30675
Status:
Mutation detected in F1 DNA
For more information about the meaning of this status and other statuses, please see our FAQs.
Availability:
Not yet available
Mutation:
C > T
Consequence:
Nonsense
Transcripts:
Transcript ID Consequence Amino Acid Affected Amino Acid Total Exon Affected Exon Total
ENSDART00000125081 Nonsense 1182 1368 26 30
Genomic Location (Zv9):
Chromosome 14 (position 19729462)
Other Location(s):
Assembly Chromosome Position
GRCz10 14 15523915
GRCz11 14 15829478
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
GGGAGAGACCCACATTTCCAGCTCTGGTGGAGATACTTGGAGATCTACTG[C/T]AGGAAAACAGTCTACCAGTGAGAAGATGCACACACACACACACATTGTGA
Long Flanking Sequence:
TCATATTTCTTAAATGATTAAAAAGTTAAGTGAACAACATTGATTTAAAATGTATATATTTGTTTATTTGTTCTAATATTTACCATTTGTAACACTTTACTATGTTTTGTATTTATATTTAATTCCATTTATGTCCAACTTCAGAGTGTTTTATGCCAGACTGAATTGTATTGTATGCCATCAGGAGCGTCTCCATACCCCGGCATCCAGATTGATGAAGATTTCTGCAAACGACTCAAAGACGGTACCAGGATGAGAGCACCAGACAATGCGTCCCCTGAAATGTGAGCAAAGTCCTGATTGCATTACATGTGTGCATGTGTTTGACTGACGGCTAATCAGACTGATGACGTCAGCCGGTGATGAAACTCTGTGAGCTACGTGTTCATGTGTTGTCGATGTGTTCTGACAGATATGGCATCATGTTGGCCTGCTGGCAGGGCGAGCCCAGGGAGAGACCCACATTTCCAGCTCTGGTGGAGATACTTGGAGATCTACTG[C/T]AGGAAAACAGTCTACCAGTGAGAAGATGCACACACACACACACATTGTGAACATTACACAAACACTGGTATCTGGATGATAGCAAGACAGCCGTTTATTAGGTTAACACTTTATTTTGATGGTCCGTTTGTTTGTTTAATTCAAGTTACATTGCCACTAATTCTCATTAGATTATAAGTAGACTGTTAGGTTGGAGTTAGGGTTAATGTAAGTTGACATGTACTTGCAAAGTTTCTTGTAGTCAGTTAAATGTCTGTTGATGGCGCAGCATCAACAGATATTAAGCAGACAGTCTACTAATGCTCAAATGCACAATCAAGTGTTACCATTTGCTATACTGTATAATATAGGATTATAGTATATAATTCAATACTATAATATATCAGTGTCAGTGTCATAATATAAGCAGTGTCAGTGCTTAAATTGAGAGGGGATGCGGGGAGATGGTATCCCCACACAACGGTGTATGTAATATAAAACTTAACAGGCAAATTAAATAT
Associated Phenotype:
Not determined